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Hearing Instability in Children with Congenital Cytomegalovirus: Evidence and Neural Consequences

The Laryngoscope, 2022-09, Vol.132 (S11), p.S1-S24

2022

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Endolymphatic hydrops in the horizontal semicircular canal: A morphologic correlate for canal paresis in Ménière's disease

The Laryngoscope, 2013-02, Vol.123 (2), p.503-506

2013

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Birt‐Hogg‐Dubé syndrome: an underdiagnosed genetic tumor syndrome

Journal der Deutschen Dermatologischen Gesellschaft, 2018-03, Vol.16 (3), p.278-283

2018

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Birt‐Hogg‐Dubé‐Syndrom: ein zu selten diagnostiziertes erbliches Tumorsyndrom

Journal der Deutschen Dermatologischen Gesellschaft, 2018-03, Vol.16 (3), p.278-284

2018

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Sarcoid-like reaction in a child following prolonged therapeutic exposure to dabrafenib and trametinib for BRAF V600E mutated hypothalamic/chiasmatic glioma

Pediatric blood & cancer, 2023-11, Vol.70 (11), p.e30619

2023

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Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa

Clinical genetics, 2022-12, Vol.102 (6), p.524-529

2022

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Influence of the compliance of the neck arteries and veins on the measurement of intracranial volume change by phase-contrast MRI

Journal of magnetic resonance imaging, 2009-10, Vol.30 (4), p.878-883

2009

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Long-term neurodevelopmental outcomes following liver transplantation for metabolic disease-a single centre experience

Journal of inherited metabolic disease, 2024-08

2024

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MRI pulmonary artery flow detects lung vascular pathology in preterms with lung disease

The European respiratory journal, 2023-12, Vol.62 (6), p.2202445

2023

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Muscle Atrophy Beyond the Clinical Effect After a Single Dose of OnabotulinumtoxinA Injected in the Procerus Muscle: A Study with Magnetic Resonance Imaging

Dermatologic surgery, 2013-05, Vol.39 (5), p.761-765

2013

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Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum

American journal of medical genetics. Part A, 2009-07, Vol.149A (7), p.1592-1594

2009

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Loss of tubulin deglutamylase CCP 1 causes infantile‐onset neurodegeneration

The EMBO journal, 2018-12, Vol.37 (23)

2018

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Effect of Photofrin II as a radio-sensitizing agent in two different oesophageal carcinoma cell lines

Journal of porphyrins and phthalocyanines, 2005-07, Vol.9 (7), p.470-475

2005

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Inter- and intra-rater reliability of blood and CSF flow quantification by phase-contrast MRI

Journal of magnetic resonance imaging, 2013-01, Vol.38 (3), p.655-662

2013

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The influence of oxygen on the radiosensitizing activity of Photofrin II and hypericin

Journal of porphyrins and phthalocyanines, 2007-10, Vol.11 (10), p.736-741

2007

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The role of radical derivatives of high reactivity in the radiosensitizing action of Photofrin II

Journal of porphyrins and phthalocyanines, 2006-12, Vol.10 (12), p.1398-1402

2006

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Anisotropy of transcallosal motor fibres indicates functional impairment in children with periventricular leukomalacia: Anisotropy of Motor Fibres in PVL

Developmental medicine and child neurology, 2011-02, Vol.53 (2), p.179-186

2011

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Maternallg Inherited Heterozygous Sequence Change in the Sonic Hedgehog Gene in a Male Patient with Bilateral Closed-Lip Schizencephaly and Partial Absence of the Corpus Callosum

American journal of medical genetics. Part A, 2009, Vol.149 (7), p.1592-1594

2009

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Agenesis andDysgenesis of the Corpus Callosum : Clinical, Genetic and Neuroimaging Findings in a Series of 41 Patients

American journal of medical genetics. Part A, 2008, Vol.146 (19), p.2501-2511

2008

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Sarcoid-like reaction in a child following prolonged therapeutic exposure to dabrafenib and trametinib for BRAF V600E mutated hypothalamic/chiasmatic glioma

Pediatric blood & cancer, 2023, Vol.70 (11), p.e30619-e30619

2023

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How doctors think--and treat with botulinum toxin

Developmental medicine and child neurology, 2010, Vol.52 (9), p.875-876

2010

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Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum

American journal of medical genetics. Part A, 2009, Vol.149A (7), p.1592-1594

2009

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Expression of appreciation: 2011 JMRI reviewers

Journal of magnetic resonance imaging, 2012-12, Vol.36 (6), p.1496-1501

2012

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Epilepsia Reviewers

Epilepsia (Copenhagen), 2005-12, Vol.46 (12), p.1849-1855

Fisher, Robert S.

2005

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Hearing Instability in Children with Congenital Cytomegalovirus: Evidence and Neural Consequences

Endolymphatic hydrops in the horizontal semicircular canal: A morphologic correlate for canal paresis in Ménière's disease

Birt‐Hogg‐Dubé syndrome: an underdiagnosed genetic tumor syndrome

Birt‐Hogg‐Dubé‐Syndrom: ein zu selten diagnostiziertes erbliches Tumorsyndrom

Sarcoid-like reaction in a child following prolonged therapeutic exposure to dabrafenib and trametinib for BRAF V600E mutated hypothalamic/chiasmatic glioma

Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa

Influence of the compliance of the neck arteries and veins on the measurement of intracranial volume change by phase-contrast MRI

Long-term neurodevelopmental outcomes following liver transplantation for metabolic disease-a single centre experience

MRI pulmonary artery flow detects lung vascular pathology in preterms with lung disease

Muscle Atrophy Beyond the Clinical Effect After a Single Dose of OnabotulinumtoxinA Injected in the Procerus Muscle: A Study with Magnetic Resonance Imaging

Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum

Loss of tubulin deglutamylase CCP 1 causes infantile‐onset neurodegeneration

Effect of Photofrin II as a radio-sensitizing agent in two different oesophageal carcinoma cell lines

Inter- and intra-rater reliability of blood and CSF flow quantification by phase-contrast MRI

The influence of oxygen on the radiosensitizing activity of Photofrin II and hypericin

The role of radical derivatives of high reactivity in the radiosensitizing action of Photofrin II

Anisotropy of transcallosal motor fibres indicates functional impairment in children with periventricular leukomalacia: Anisotropy of Motor Fibres in PVL

Maternallg Inherited Heterozygous Sequence Change in the Sonic Hedgehog Gene in a Male Patient with Bilateral Closed-Lip Schizencephaly and Partial Absence of the Corpus Callosum

Agenesis andDysgenesis of the Corpus Callosum : Clinical, Genetic and Neuroimaging Findings in a Series of 41 Patients

Sarcoid-like reaction in a child following prolonged therapeutic exposure to dabrafenib and trametinib for BRAF V600E mutated hypothalamic/chiasmatic glioma

How doctors think--and treat with botulinum toxin

Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum

Expression of appreciation: 2011 JMRI reviewers

Epilepsia Reviewers

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